A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4203806



Internal ID11139658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:202205209..202205415hg38UCSC Ensembl
chr1:202174337..202174543hg19UCSC Ensembl
chr1:200440960..200441166hg18UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38207
hg19207
hg18207
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1257220
Supporting Variants
SamplesHuRef
Known GenesLGR6
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4203806
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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